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Genetics of Prader-Willi syndrome

Resumen/Descripción – provisto por la editorial

No disponible.

Palabras clave – provistas por la editorial

Prader-Willi syndrome; appetite treatment; Caralluma fimbriata extract; single-case; Prader–Willi syndrome; thromboembolism; risk factors; vasculitis; blood clots; registry; natural history; age diagnosis; obesity; deletion; uniparental disomy; genetic syndrome; mental illness; psychosis; major depressive illness; obsessive-compulsive disorder; autism; eating disorder; skin picking; insurance health claims; thrombosis; pulmonary embolism; deep venous thrombosis; individuals with exogenous obesity; confirmatory ICD-9 diagnostic codes; Prader–Willi; 15q11.2; SNORD116; atypical microdeletion; food-related behavior; childhood; scoliosis; kyphosis; spinal deformities; junctional kyphosis; treatment options; surgery; bracing; KATP channel activation; hyperphagic obesity; animal models; weight; BMI; pediatric; linear mixed models; gut microbiota; bacteria; fungi; diet; hyperphagia; cross-sectional; games; parents; home; exercise; bone health; Prader-Willi syndrome (PWS); PWS molecular classes; PWS genetic subtype–phenotype correlations; psychiatric behavioral phenotype; growth hormone treatment; pharmacogenetic testing; cytochrome P450 enzymes; drug interactions; medication management; n/a

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Información

Tipo de recurso:

libros

ISBN electrónico

978-3-0365-5026-8

País de edición

Suiza